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dc.contributor.authorPan, Q.
dc.contributor.authorPetit-Frere, C.
dc.contributor.authorStavnezer, Janet
dc.contributor.authorHammarstrom, L.
dc.date2022-08-11T08:11:04.000
dc.date.accessioned2022-08-23T17:31:09Z
dc.date.available2022-08-23T17:31:09Z
dc.date.issued2000-04-01
dc.date.submitted2007-09-14
dc.identifier.citation<p>Eur J Immunol. 2000 Apr;30(4):1019-29.</p>
dc.identifier.issn0014-2980 (Print)
dc.identifier.doi10.1002/(SICI)1521-4141(200004)30:4<1019::AID-IMMU1019>3.0.CO;2-W
dc.identifier.pmid10760789
dc.identifier.urihttp://hdl.handle.net/20.500.14038/50667
dc.description.abstractThe mechanism underlying the differential regulation of switching to human IgG subclasses is still largely unknown. We demonstrate that the region upstream of the initiation sites for gamma3 germ-line (GL) transcripts contains a functional promoter which is synergistically induced by IL-4, antibody to CD40 and phorbol dibutyrate in transient transfection assays in the human DG75 cell line. Linker-scanning mutations identified multiple elements in the 3' half of the evolutionarily conserved sequence that are required for inducibility. Electrophoretic mobility shift assays showed that Stat6 and NF-kappaB p50 / p65 are induced after stimulation, and bind to specific sequence motifs within the promoter. Overexpression of Stat6, NF-kappaB p50 / p65 and C / EBPgamma synergistically induced the GL gamma3 promoter. Insertion of DNA segments from the human 3' IgH regions, which may function as a locus control region for switch recombination, greatly activated the promoter in an orientation-independent manner. Duplication of the enhancer fragments resulted in a further increase of promoter activity. The greater enhancement of the HS1,2 fragment from the 3' alpha1 rather than the alpha2 locus may suggest a mechanistic explanation for the differential expression of various isotypes.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10760789&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1002/(SICI)1521-4141(200004)30:4<1019::AID-IMMU1019>3.0.CO;2-W
dc.subjectAntigens, CD40
dc.subjectB-Lymphocytes
dc.subjectBase Sequence
dc.subjectCCAAT-Enhancer-Binding Proteins
dc.subjectDNA
dc.subjectDNA-Binding Proteins
dc.subjectDrug Synergism
dc.subjectEnhancer Elements (Genetics)
dc.subjectGenes, Immunoglobulin
dc.subjectHumans
dc.subjectImmunoglobulin Class Switching
dc.subjectImmunoglobulin G
dc.subjectInterleukin-4
dc.subjectMolecular Sequence Data
dc.subjectMutagenesis, Insertional
dc.subjectNF-kappa B
dc.subjectNuclear Proteins
dc.subjectPhorbol 12,13-Dibutyrate
dc.subjectPromoter Regions (Genetics)
dc.subjectRNA, Messenger
dc.subjectResponse Elements
dc.subjectSTAT6 Transcription Factor
dc.subjectTrans-Activation (Genetics)
dc.subjectTrans-Activators
dc.subjectTranscription, Genetic
dc.subjectTumor Cells, Cultured
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectWomen's Studies
dc.titleRegulation of the promoter for human immunoglobulin gamma3 germ-line transcription and its interaction with the 3'alpha enhancer
dc.typeJournal Article
dc.source.journaltitleEuropean journal of immunology
dc.source.volume30
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/192
dc.identifier.contextkey367653
html.description.abstract<p>The mechanism underlying the differential regulation of switching to human IgG subclasses is still largely unknown. We demonstrate that the region upstream of the initiation sites for gamma3 germ-line (GL) transcripts contains a functional promoter which is synergistically induced by IL-4, antibody to CD40 and phorbol dibutyrate in transient transfection assays in the human DG75 cell line. Linker-scanning mutations identified multiple elements in the 3' half of the evolutionarily conserved sequence that are required for inducibility. Electrophoretic mobility shift assays showed that Stat6 and NF-kappaB p50 / p65 are induced after stimulation, and bind to specific sequence motifs within the promoter. Overexpression of Stat6, NF-kappaB p50 / p65 and C / EBPgamma synergistically induced the GL gamma3 promoter. Insertion of DNA segments from the human 3' IgH regions, which may function as a locus control region for switch recombination, greatly activated the promoter in an orientation-independent manner. Duplication of the enhancer fragments resulted in a further increase of promoter activity. The greater enhancement of the HS1,2 fragment from the 3' alpha1 rather than the alpha2 locus may suggest a mechanistic explanation for the differential expression of various isotypes.</p>
dc.identifier.submissionpathwfc_pp/192
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.source.pages1019-29


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